ONTOLOGY REPORT - ANNOTATIONS


Term:Marsden Syndrome
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Accession:DOID:9008398 term browser browse the term
Synonyms:exact_synonym: Dystonia, familial, with visual failure and striatal lucencies;   Leber Hereditary Optic Neuropathy With Dystonia
 primary_id: MESH:C536024;   RDO:0001435
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Marsden Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mt-nd1 mitochondrially encoded NADH dehydrogenase 1 JBrowse link MT 2,740 3,694 RGD:8554872
G Mt-nd3 mitochondrially encoded NADH dehydrogenase 3 JBrowse link MT 9,451 9,798 RGD:8554872
G Mt-nd4 mitochondrially encoded NADH dehydrogenase 4 JBrowse link MT 10,160 11,537 RGD:8554872
G Mt-nd6 mitochondrially encoded NADH dehydrogenase 6 JBrowse link MT 13,543 14,061 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14875
    syndrome 4220
      Marsden Syndrome 4
Path 2
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      nervous system disease 9116
        peripheral nervous system disease 2009
          neuropathy 1830
            cranial nerve disease 356
              optic nerve disease 186
                optic atrophy 89
                  Hereditary Optic Atrophies 57
                    Leber hereditary optic neuropathy 24
                      Marsden Syndrome 4
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